Canonical Allele Identifier: CA819008859
Gene: ARG1 HGNC NCBI

Linked Data

dbSNP Id: rs1392116192

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131573159C>T , CM000668.2:g.131573159C>T GRCh38
NC_000006.11:g.131894299C>T , CM000668.1:g.131894299C>T GRCh37
NC_000006.10:g.131935992C>T NCBI36
NG_007086.2:g.4935C>T
NG_031860.1:g.60065G>A
NG_031860.2:g.60065G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000672052.1:n.305-3504C>T
ENST00000672233.1:c.77-5952C>T ENSP00000499826.1:n.77-5952C>T
ENST00000673234.1:c.77-3504C>T ENSP00000499885.1:n.77-3504C>T
ENST00000368087.7:c.-124C>T ENSP00000357066.3:n.-124C>T
XM_011535801.2:c.-124C>T XP_011534103.1:n.-124C>T